Document Detail


Ross syndrome plus: beyond horner, Holmes-Adie, and harlequin.
MedLine Citation:
PMID:  11134383     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Ross syndrome is an uncommon disorder characterized by the triad of segmental anhidrosis, hyporeflexia, and tonic pupils. METHODS: The authors describe the clinical findings of five patients with Ross syndrome and detail the results of their pharmacologic and autonomic testing. RESULTS: In four patients, the classic findings of Ross syndrome were accompanied by Horner's syndrome. Other symptoms of dysautonomia were also common. CONCLUSIONS: These findings suggest that Ross syndrome is a dysautonomic condition of varying expression resulting from a generalized injury to ganglion cells or their projections.
Authors:
R K Shin; S L Galetta; T Y Ting; K Armstrong; S J Bird
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Neurology     Volume:  55     ISSN:  0028-3878     ISO Abbreviation:  Neurology     Publication Date:  2000 Dec 
Date Detail:
Created Date:  2001-01-08     Completed Date:  2001-02-01     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0401060     Medline TA:  Neurology     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1841-6     Citation Subset:  AIM; IM    
Affiliation:
Departments of Neurology, Hospital of the University of Pennsylvania, Philadelphia 19104-4283, USA. shirobk@mail.med.upenn.edu
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Adult
Female
Heart Rate / physiology
Horner Syndrome / physiopathology*
Humans
Hypohidrosis / physiopathology*
Male
Middle Aged
Parasympathetic Fibers, Postganglionic / physiopathology*
Sweating / physiology*
Syndrome

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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